Yv. Bobryshev et Rsa. Lord, MAPPING OF VASCULAR DENDRITIC CELLS IN ATHEROSCLEROTIC ARTERIES SUGGESTS THEIR INVOLVEMENT IN LOCAL IMMUNE-INFLAMMATORY REACTIONS, Cardiovascular Research, 37(3), 1998, pp. 799-810
Objective: We previously demonstrated that vascular dendritic cells (V
DCs) are present in the intima of large arteries and that their number
s are increased in atherosclerotic lesions. This study was undertaken
to determine whether VDC are involved in immune-mediated reactions in
atherogenesis. Methods: Specimens of carotid artery and aorta were obt
ained at operation. VDCs were identified with anti-CD1a or with S-100.
Co-localisation of VDCs with different intimal cells, including T-cel
ls and macrophages, was studied using a double immunostaining procedur
e. In areas where the co-localising cells were detected, the peculiari
ties of expression of HLA-DR, ICAM-1, VCAM-1 were examined. Results: I
n all the atherosclerotic plaques, VDCs were seen in contact with T-ce
lls, but these co-localising cells were irregularly distributed and we
re mainly found in zones of neovascularisation containing inflammatory
infiltrates. In other areas, T-cell/VDC co-localisation was rarely de
tected but VDCs were often found in contact with macrophages. VDCs wer
e detected also in the media beneath atherosclerotic lesions and in th
e adventitia, where they were mostly around vasa vasorum, especially i
n areas exhibiting signs of acute inflammation. In these areas VDCs ex
pressed ICAM-1, VCAM-1 and were in contact with T-cells. In both plaqu
es and in the adventitia, the areas with co-localising VDCs and T-cell
s corresponded to the areas with HLA-DR expression. Conclusions: The r
esults suggest that VDCs are involved in T-cell activation in atheroge
nesis. There are two regions within the arterial wall where VDC/T-cell
co-localisation mostly occurs, namely, in zones of neovascularisation
containing inflammatory infiltrates located within atherosclerotic le
sions, and in areas with inflammatory infiltrates around vasa vasorum
in the adventitia. Possibly, some intimal VDCs migrate through the med
ia and adventitia to adjacent lymph nodes where they present atheroscl
erosis associated antigens. We also speculate that VDC/macrophage cont
acts are essential in processing immune information in atherogenesis.
(C) 1998 Elsevier Science B.V.